A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699964



Internal ID15089930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55107562..55755073hg38UCSC Ensembl
Innerchr11:54875038..55522549hg19UCSC Ensembl
Innerchr11:54631614..55279125hg18UCSC Ensembl
Innerchr11:54631614..55279125hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38647512
hg19647512
hg18647512
hg17647512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524091
Supporting Variants
Samples
Known GenesOR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, TRIM48, TRIM51HP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699964
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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